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保加利亚多囊肾病的遗传异质性。

Genetic heterogeneity of polycystic kidney disease in Bulgaria.

作者信息

Bogdanova N, Dworniczak B, Dragova D, Todorov V, Dimitrakov D, Kalinov K, Hallmayer J, Horst J, Kalaydjieva L

机构信息

Institut für Humangenetik der Universität, Münster, Germany.

出版信息

Hum Genet. 1995 Jun;95(6):645-50. doi: 10.1007/BF00209481.

Abstract

Linkage analysis was performed on 22 Bulgarian families with polycystic kidney disease (PKD) ascertained through the hemodialysis centers of two medical schools. A total of 128 affected and 59 unaffected individuals, and 54 spouses have been investigated using eight polymorphic markers linked to PKD1 and nine markers to PKD2. The results demonstrate locus heterogeneity with 0.67 as the maximum likelihood value of alpha, i.e., the proportion of families linked to PKD1. In five families, the results suggest linkage to PKD2 and observed recombinants place the gene between loci D4S1544 and D4S1542. In one family, two double recombinants for closely linked markers on chromosome 16 and on chromosome 4 give evidence for the lack of linkage to either PKD1 or PKD2, thus suggesting the involvement of a third locus. Analysis of clinical data in the PKD1 group versus the unlinked group shows no significant differences in the severity of the disease.

摘要

对通过两所医学院的血液透析中心确诊的22个患有多囊肾病(PKD)的保加利亚家庭进行了连锁分析。使用与PKD1连锁的8个多态性标记和与PKD2连锁的9个标记,对总共128名患病个体、59名未患病个体以及54名配偶进行了调查。结果表明存在基因座异质性,α的最大似然值为0.67,即与PKD1连锁的家庭比例。在5个家庭中,结果提示与PKD2连锁,观察到的重组体将该基因定位于基因座D4S1544和D4S1542之间。在1个家庭中,16号染色体和4号染色体上紧密连锁标记的两个双重组体证明与PKD1或PKD2均无连锁,从而提示存在第三个基因座的参与。PKD1组与非连锁组的临床数据分析显示,疾病严重程度无显著差异。

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